光生物调节治疗腕管释放:一项随机对照试验。

Jia Peng Chuah, Saw Sian Khoo, Tze Yang Chung, Gunasagaran Jayaletchumi
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引用次数: 0

摘要

背景:腕管释放术(Carpal tunnel release, CTR)被广泛认为是治疗腕管综合征的有效方法。然而,恢复往往是延迟的和不完整的。光生物调节疗法(PBMT)对活组织产生非热效应;它促进愈合,重塑和减少受伤神经的炎症。本研究的目的是比较术后行PBMT和未行PBMT患者的CTR结果。材料和方法:我们从2019年1月至2021年1月招募了105例开放式CTR患者。56例患者符合研究标准,随机分为两组:服用PBMT (n = 28)和不服用PBMT (n = 28)。术前获得人口学和临床资料。PBMT组在3周内使用808 nm, 50 mW的PBMT进行10次3分钟的治疗,每次治疗向CTR切口疤痕输送9 J。分别于术后1、3、6个月评估临床结果。采用SPSS软件进行数据分析。结果:与非PBMT组相比,PBMT组术后1个月的波士顿腕管问卷功能状态量表(p = 0.018)和早晨疼痛(视觉模拟量表)(p = 0.019)均有显著改善。PBMT组在3个月(p = 0.022)、6个月(p = 0.024)、1个月(p = 0.042)、3个月(p = 0.05)、3个月(p = 0.005)时针尖夹紧强度的改善明显优于对照组。PBMT组在3个月(p = 0.018)和6个月(p = 0.016)时的拇指2点辨别能力(2PD)和3个月时的食指2点辨别能力(p = 0.039)也有显著改善。PBMT无副作用报道。结论:ctr后接受PBMT治疗的患者预后较好。PBMT可能是一个有价值的辅助治疗后治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photobiomodulation Therapy in Carpal Tunnel Release: A Randomized Controlled Trial.

Background: Carpal tunnel release (CTR) is widely accepted as an effective treatment for carpal tunnel syndrome. However, the recovery is often delayed and incomplete. Photobiomodulation therapy (PBMT) produces a nonthermal effect on living tissues; it promotes healing, remodels and reduces inflammation of an injured nerve. The purpose of this study was to compare the outcome of CTR between patients who underwent postoperative PBMT and without PBMT. Materials and methods: We recruited 105 patients who had open CTR from January 2019 to January 2021. Fifty-six patients fulfilled the study criteria and were randomized into two groups: with PBMT (n = 28) and without PBMT (n = 28). Demographic and clinical data were obtained preoperatively. The PBMT group had ten 3-min sessions over 3 weeks using 808 nm, 50 mW PBMT to deliver 9 J per session to the CTR incision scar. Clinical outcomes were assessed at 1, 3, and 6 months postoperatively. Data analysis was performed with SPSS software. Results: There were significant improvements in the Functional Status Scale in the Boston Carpal Tunnel Questionnaire (p = 0.018) and pain (visual analogue scales) in the morning (p = 0.019) at 1 month postoperatively in the PBMT group compared with the non-PBMT group. Improvement of tip pinch strength at 3 months (p = 0.022) and 6 months (p = 0.024), lateral pinch strength at 1 month (p = 0.042) and 3 months (p = 0.05), and tripod pinch strength at 3 months (p = 0.005) was significantly better in the PBMT group. Thumb 2-point discrimination (2PD) at 3 months (p = 0.018) and 6 months (p = 0.016) and index finger 2PD at 3 months (p = 0.039) were also significantly improved in the PBMT group. There were no side effects of PBMT reported. Conclusions: Patients who underwent PBMT post-CTR had better outcomes. PBMT may be a valuable adjunct to post-CTR care.

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